A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17597268



Internal ID21789311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:25504979..25523237hg38UCSC Ensembl
chr10:25793908..25812166hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3818259
hg1918259
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6003800
Supporting Variants
Samples
Known GenesGPR158
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17597268
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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